Monitoring the expression pattern of 1300 Arabidopsis genes under drought and cold stresses by using a full-length cDNA microarray

被引:811
作者
Seki, M
Narusaka, M
Abe, H
Kasuga, M
Yamaguchi-Shinozaki, K
Carninci, P
Hayashizaki, Y
Shinozaki, K
机构
[1] RIKEN, Genom Sci Ctr, Plant Funct Genomics Res Grp, Plant Mutat Explorat Team, Tsukuba, Ibaraki 3050074, Japan
[2] RIKEN, Tsukuba Inst, Plant Mol Biol Lab, Tsukuba, Ibaraki 3050074, Japan
[3] Minist Agr Forestry & Fisheries, Japan Int Res Ctr Agr Sci, Biol Resources Div, Tsukuba, Ibaraki 3050851, Japan
[4] RIKEN, Tsukuba Inst, Genome Sci Lab, Tsukuba, Ibaraki 3050074, Japan
关键词
D O I
10.1105/tpc.13.1.61
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pull-length cDNAs are essential for functional analysis of plant genes, Using the biotinylated CAP trapper method, we constructed full-length Arabidopsis cDNA libraries from plants in different conditions, such as drought-treated, cold-treated, or unstressed plants, and at various developmental stages from germination to mature seed. We prepared a cDNA microarray using similar to 1300 full-length Arabidopsis cDNAs to identify drought- and cold-inducible genes and target genes of DREB1A/CBF3, a transcription factor that controls stress-inducible gene expression, In total, 44 and 19 cDNAs for drought- and cold-inducible genes, respectively, were isolated, 30 and 10 of which were novel stress-inducible genes that have not been reported as drought- or cold-inducible genes previously, Twelve stress-inducible genes were identified as target stress-inducible genes of DREB1A, and six of them were novel, On the basis of RNA gel blot and microarray analyses, the six genes were identified as novel drought- and cold-inducible genes that are controlled by DREB1A, Eleven DREB1A target genes whose genomic sequences have been registered in the GenBank database contained the dehydration-responsive element (DRE) or DRE-related CCGAC core motif in their promoter regions. These results show that our full-length cDNA microarray is a useful material with which to analyze the expression pattern of Arabidopsis genes under drought and cold stresses, to identify target genes of stress-related transcription factors, and to identify potential cis-acting DNA elements by combining the expression data with the genomic sequence data.
引用
收藏
页码:61 / 72
页数:12
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